Rapid mobilization of murine hematopoietic stem cells with enhanced engraftment properties and evaluation of hematopoietic progenitor cell mobilization in rhesus monkeys by a single injection of SB-251353, a specific truncated form of the human CXC chemokine GROβ
Open Access
- 15 March 2001
- journal article
- research article
- Published by American Society of Hematology in Blood
- Vol. 97 (6) , 1534-1542
- https://doi.org/10.1182/blood.v97.6.1534
Abstract
SB-251353 is an N-terminal truncated form of the human CXC chemokine GROβ. Recombinant SB-251353 was profiled in murine and rhesus monkey peripheral blood stem cell mobilization and transplantation models. SB-251353 rapidly and transiently mobilized hematopoietic stem cells and neutrophils into the peripheral blood after a single subcutaneous injection. Transplantation of equivalent numbers of hematopoietic stem cells mobilized by SB-251353 into lethally irradiated mice resulted in faster neutrophil and platelet recovery than stem cells mobilized by granulocyte colony-stimulating factor (G-CSF). A single injection of SB-251353 in combination with 4 days of G-CSF administration resulted in augmented stem and progenitor cell mobilization 5-fold greater than G-CSF alone. Augmented stem cell mobilization could also be demonstrated in mice when a single injection of SB-251353 was administered with only one-day treatment with G-CSF. In addition, SB-251353, when used as a single agent or in combination with G-CSF, mobilized long-term repopulating stem cells capable of hematopoietic reconstitution of lethally irradiated mice. In rhesus monkeys, a single injection of SB-251353 induced rapid increases in peripheral blood hematopoietic progenitor cells at a 50-fold lower dose than in mice, which indicates a shift in potency. These studies provide evidence that the use of SB-251353 alone or in combination with G-CSF mobilizes hematopoietic stem cells with long-term repopulating ability. In addition, this treatment may (1) reduce the number of apheresis sessions and/or amount of G-CSF required to collect adequate numbers of hematopoietic stem cells for successful peripheral blood cell transplantation and (2) improve hematopoietic recovery after transplantation.Keywords
This publication has 47 references indexed in Scilit:
- The utilization of cytokines in stem cell mobilization strategiesBone Marrow Transplantation, 1999
- Biology of IL‐8‐Induced Stem Cell MobilizationAnnals of the New York Academy of Sciences, 1999
- Peripheral Blood Stem Cell Mobilization for High-Dose ChemotherapyJournal of Hematotherapy, 1999
- Effects of CC, CXC, C, and CX3C Chemokines on Proliferation of Myeloid Progenitor Cells, and Insights into SDF‐1‐Induced Chemotaxis of ProgenitorsaAnnals of the New York Academy of Sciences, 1999
- A functional granulocyte colony-stimulating factor receptor is required for normal chemoattractant-induced neutrophil activationJournal of Clinical Investigation, 1999
- Blockade of CC chemokine receptor 5 (CCR5)-tropic human immunodeficiency virus-1 replication in human lymphoid tissue by CC chemokines.Journal of Clinical Investigation, 1998
- Optimal timing for collection of PBPC after glycosylated G-CSF administrationBone Marrow Transplantation, 1998
- Effect of interleukin‐3 pretreatment on granulocyte/macrophage colony‐stimulating factor induced mobilization of circulating haemopoietic progenitor cellsBritish Journal of Haematology, 1995
- Mobilization of long-term reconstituting hematopoietic stem cells in mice by recombinant human interleukin 7.The Journal of Experimental Medicine, 1995
- Inhibition of Matrix Metalloproteinase 9 Activation by a Specific Monoclonal AntibodyHybridoma, 1993